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dc.contributor.author
Zacur Vercellone, Sofia Susana
dc.contributor.author
Sham, Edgardo Ling
dc.contributor.author
Farfan Torres, Elsa Monica
dc.date.available
2017-08-10T19:41:11Z
dc.date.issued
2015-09
dc.identifier.citation
Zacur Vercellone, Sofia Susana; Sham, Edgardo Ling; Farfan Torres, Elsa Monica; Caracterización superficial y textural de organoarcillas pilareadas con TiO2; Universidade Federal do Rio de Janeiro. Coordenação dos Programas de Pós-Graduação em Engenharia. Laboratório de Hidrogênio; Revista Matéria; 20; 3; 9-2015; 755-763; 11647
dc.identifier.issn
1517-7076
dc.identifier.uri
http://hdl.handle.net/11336/22130
dc.description.abstract
TiO2 organoclays are potential adsorbents for aqueous pollutants and subsequently they could favour the photocatalysis of them. For this reason, the study of their surface and textural characteristics is important for the improvement of those processes. In this work TiO2 pillared organoclays were studied. The surfactant (hexadecyltrimethilammonium bromide) was introduced post-pillaring or during the pillaring process. The effect of the use of different acids of hydrolysis and different surfactants ratios was investigated. The clays were characterized by thermogravimetric analysis, infrared spectroscopy and nitrogen sorptometry. It was found that the highest adsorption capacity post-pillaring of the surfactant is near to 0.5 times the CEC of the original pillared clay, independently of the amount of surfactant offered. An increment in the amount of the surfactant introduced only increased the ratio adsorbed as ionic pair. In these samples the CEC measured after the adsorption was between 0.26 and 0.47 times the original CEC. It was observed a decrease in the total pore volume and the BET surface for every sample. The surface hydrophobicity of the samples with post-pillaring adsorption was higher than in those with co-adsorption. In conclusion, it was demonstrated that the incorporation of surfactant modifies the surface and textural properties of the material in different extent in accordance with the incorporation stage and the amount of surfactant used.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Universidade Federal do Rio de Janeiro. Coordenação dos Programas de Pós-Graduação em Engenharia. Laboratório de Hidrogênio
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Organoclays
dc.subject
Pillared Clays
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Textural Properties
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Surface Hydrophobicity
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Compuestos
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Ingeniería de los Materiales
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INGENIERÍAS Y TECNOLOGÍAS
dc.title
Caracterización superficial y textural de organoarcillas pilareadas con TiO2
dc.title
Surface and textural characterization of TiO2 pillared organoclays
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2016-12-16T16:42:04Z
dc.journal.volume
20
dc.journal.number
3
dc.journal.pagination
755-763; 11647
dc.journal.pais
Brasil
dc.journal.ciudad
Rio de Janeiro
dc.description.fil
Fil: Zacur Vercellone, Sofia Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones Para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones Para la Industria Química; Argentina
dc.description.fil
Fil: Sham, Edgardo Ling. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones Para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones Para la Industria Química; Argentina
dc.description.fil
Fil: Farfan Torres, Elsa Monica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones Para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones Para la Industria Química; Argentina
dc.journal.title
Revista Matéria
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1590/S1517-707620150003.0080
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://ref.scielo.org/wkzkj9
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